Clinical Trial Manager

i-Pharm Consulting; London; Hybrid; GBP 60,000 - 90,000; Full time

Benefits offered by this job

Competitive package

Career growth opportunities

Flexible onsite attendance

Job summary

A leading sponsor client in London is seeking a Clinical Trial Manager for managing Phase Ib-III virology clinical trials. The role involves coordinating study documents, managing CROs, and ensuring compliance. Ideal candidates should have clinical trial management experience and a relevant scientific background. Competitive package offered along with flexible onsite attendance.

Qualifications

• Proven clinical trial management experience at senior CTMA level.
• Relevant scientific background (BSc or nursing qualification).
• Familiarity with FDA, EU regulations, ICH guidelines, and GCP.
• Experience with virology studies advantageous but not essential.
• Strong organizational, communication, and teamwork skills.

Responsibilities

• Manage regional components of global studies ensuring timely delivery.
• Coordinate study documents including protocols and monitoring plans.
• Manage CROs/vendors and train study teams on protocol adherence.
• Support study monitoring/co-monitoring and regulatory compliance.
• Collaborate closely with stakeholders to ensure study progress.

Skills

Clinical trial management

Organizational skills

Communication

Teamwork

Multitasking

Education

BSc or nursing qualification

Job description

Clinical Trial Manager – Virology | London (3-5 Days Onsite)

Join a leading sponsor client driving cutting-edge Phase Ib-III virology clinical trials across the EMEA region on a 12 month contracted role . As Clinical Trial Manager, you will play a pivotal role in managing regional components of global studies, ensuring timely delivery and quality execution in partnership with CROs and cross-functional teams.

Key Responsibilities:

• Regional management of Phase Ib-III clinical trials for a sponsor client
• Coordination of study documents including protocols, informed consents, monitoring plans
• Manage CROs/vendors and train study teams on protocol adherence
• Support study monitoring/co-monitoring and regulatory compliance
• Collaborate closely with global and local stakeholders to ensure study progress
• Assist in study budgeting, SOP implementation, and troubleshooting

What We’re Looking For:

• Proven clinical trial management experience at senior CTMA level
• Relevant scientific background (BSc or nursing qualification)
• Familiarity with FDA, EU regulations, ICH guidelines, and GCP
• Experience with virology studies advantageous but not essential
• Strong organizational, communication, and teamwork skills
• Ability to multitask and adapt in a fast-paced environment
• Willingness for occasional international travel

Why Join?

• Work for a prestigious sponsor client with a global impact
• Lead and influence multiple virology clinical studies
• Competitive package and career growth opportunities
• Located in central London with flexible onsite attendance (3-5 days/week)

Interested? Contact us today for a confidential discussion or apply now!

Seniority level

• Seniority level

  Mid-Senior level

Employment type

• Employment type

  Contract

Job function

• Job function

  Science and Health Care Provider

• Industries

  Biotechnology Research and Pharmaceutical Manufacturing

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